Canonical Allele Identifier: CA337203

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116775088A>G , CM000669.2:g.116775088A>G	GRCh38
NC_000007.13:g.116415142A>G , CM000669.1:g.116415142A>G	GRCh37
NC_000007.12:g.116202378A>G	NCBI36
NG_008996.1:g.107684A>G , LRG_662:g.107684A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3236A>G MANE Select	NP_000236.2:p.His1079Arg
ENST00000397752.8:c.3236A>G MANE Select	ENSP00000380860.3:p.His1079Arg
NM_000245.2:c.3236A>G	NP_000236.2:p.His1079Arg
NM_000245.3:c.3236A>G	NP_000236.2:p.His1079Arg
NM_001127500.1:c.3290A>G , LRG_662t1:c.3290A>G	NP_001120972.1:p.His1097Arg
NM_001127500.2:c.3290A>G	NP_001120972.1:p.His1097Arg
NM_001127500.3:c.3290A>G	NP_001120972.1:p.His1097Arg
NM_001324402.1:c.1946A>G	NP_001311331.1:p.His649Arg
NM_001324402.2:c.1946A>G	NP_001311331.1:p.His649Arg
ENST00000318493.10:c.3290A>G	ENSP00000317272.6:p.His1097Arg
ENST00000318493.11:c.3290A>G	ENSP00000317272.6:p.His1097Arg
ENST00000397752.7:c.3236A>G	ENSP00000380860.3:p.His1079Arg
ENST00000436117.3:c.*841A>G	ENSP00000410980.2:n.*841A>G
XM_006715990.2:c.1946A>G	XP_006716053.1:p.His649Arg
XM_006715991.2:c.1946A>G	XP_006716054.1:p.His649Arg
XM_011516223.1:c.3293A>G	XP_011514525.1:p.His1098Arg
XR_001744772.1:n.3367A>G